EP1754743B1 - Flexible Polymergegenstände zur Änderung der Zähigkeit eines Prepregs - Google Patents

Flexible Polymergegenstände zur Änderung der Zähigkeit eines Prepregs Download PDF

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EP1754743B1
EP1754743B1 EP06076672.2A EP06076672A EP1754743B1 EP 1754743 B1 EP1754743 B1 EP 1754743B1 EP 06076672 A EP06076672 A EP 06076672A EP 1754743 B1 EP1754743 B1 EP 1754743B1
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Prior art keywords
resin
fibres
curable composition
flexible polymer
polymer
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French (fr)
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EP1754743A1 (de
Inventor
Carmelo c/o Cytec Fiberite Limited Lo Faro
Jeffery Thomas c/o ICI Strategic Tech. G. Carter
Patrick Terence Cytec Fiberite Limited McGrail
Robin Kelvin c/o Cytec Fiberite Inc. Maskell
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Cytec Technology Corp
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Cytec Technology Corp
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Priority claimed from GB0020630A external-priority patent/GB0020630D0/en
Priority claimed from GB0104947A external-priority patent/GB0104947D0/en
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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/04—Reinforcing macromolecular compounds with loose or coherent fibrous material
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00—Processes of treating or compounding macromolecular substances
    • C08J3/24—Crosslinking, e.g. vulcanising, of macromolecules
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/24—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs
    • C08J5/247—Impregnating materials with prepolymers which can be polymerised in situ, e.g. manufacture of prepregs using fibres of at least two types

Definitions

  • the present invention relates to a curable composition comprising at least one flexible polymer element and a curable matrix resin, and a method for preparation thereof.
  • the invention relates to a curable composition
  • a curable composition comprising a flexible polymer element as defined in the form of a fibre, film or the like, method for the preparation thereof.
  • Fibre-reinforced resin matrix composites are widely accepted for use as high strength low weight engineering materials to replace metals in aircraft structural applications and the like. These composite materials may be made by laminating prepregs comprising high strength fibres, such as glass, graphite (carbon), boron or the like impregnated with a matrix of typically thermoplastic resin. Important properties of such composites are high strength and stiffness and reduced weight.
  • Composites must meet very stringent requirements in terms of those properties which are significant in or will affect the safety of the structure comprising the composite when subject to environmental conditions including extremes of temperature (thermal cycling resistance), exposure to ultraviolet and other radiation types, exposure to atmospheric oxygen (oxidation resistance) exposure to moisture and the like; and additionally when subject to hazards such as exposure to solvents etc, in addition to the usual requirements to withstand all conceivable load and stress types, resist delamination, fracture and the like.
  • Curable compositions comprising a blend of polymer resins and optionally additionally comprising reinforcing fibres are characterised by individual physical and chemical properties of the constituent polymer resins and fibres, whereby compositions may be selected for a specific use.
  • a thermoset resin component is present which confers high solvent resistance, thermal cycling resistance etc.
  • a thermoplast resin component is present which confers high level of toughness etc, and reinforcing fibres are present which confer high levels of stiffness, for reduced weight etc.
  • the respective resins and the fibres are blended or shaped in suitable manner and cured, and retain their distribution or shape by physical and in some cases by chemical interaction in a desired end product. Nevertheless the blending or shaping is in many cases complicated by factors such as high viscosity of resins, particularly when it is desired to impregnate reinforcing fibres, a short “pot life” (pre-gelling time), obtaining uniform or selective dispersion and the like.
  • LM Liquid Moulding
  • Liquid Moulding is a generic term which covers processing techniques such as Resin Transfer Moulding (RTM), Liquid Resin Infusion (LRI), Resin Infusion Flexible Tooling (RIFT), Vacuum Assisted Resin Transfer Moulding (VARTM), Resin Film Infusion (RFI) and the like.
  • RTM Resin Transfer Moulding
  • LRI Liquid Resin Infusion
  • RIFT Resin Infusion Flexible Tooling
  • VARTM Vacuum Assisted Resin Transfer Moulding
  • RFI Resin Film Infusion
  • the potential benefits that LM has to offer over that of a conventional prepreg route are reduced scrap, reduced lay-up time, a non-dependence on tack and drape and increased shelf life properties.
  • LM technology finds its greatest use in specialised operations in which complex composite structures (multi components) are required, locally strengthened structures are required by selectively distributing carbon fibres in the mould and where the need for very large structures is required e.g. marine applications.
  • Resin Film Infusion combines an LM technology with conventional prepreg, e.g. in RTM or RFI autoclave curing, individual prepregs are stacked in a prescribed orientation to form a laminate, the laminate is laid against a smooth metal plate and covered with successive layers of porous teflon, bleeder fabric and vacuum bag. A consolidating pressure is applied to the laminate, to consolidate the individual layers and compress bubbles of any volatile that remain.
  • the use of autoclave creates a limit to the size of the components that is possible to produce. Currently for example is not possible to build a boat hull, a yacht or a bridge using an autoclave because that would require a huge pressurized autoclave adding enormous capital costs and running costs.
  • VARTM simplifies hard mold RTM by employing only one-sided moulds, and using vacuum bagging techniques to compress the preform. However mould filling times can be far too long, if indeed the resin does not cure before total fill.
  • RIFT provides much faster fill times.
  • a 'distribution media' being a porous layer having very low flow resistance, provides the injected resin with a relatively easy flow path.
  • the resin flows quickly through the distribution media, which is placed on the top of the laminate and then flows down through the thickness of the preform.
  • the use of fibres to create channels for the resin infusion is known ( WO0102146A1 (Plastech ), US5484642 (Brochier ), US5326462 (Seemann )) however these remove the channels are either removed during the degassing and curing stage or if they are left in they remain intact post cure.
  • a common disadvantage concerning the prepreg and LM technologies is in the area of very tough composite materials.
  • Resin systems which have high impact performance usually contain thermoplastic toughening agents or the like which increase the viscosity and elastic properties of the resin making it very difficult to impregnate or inject. High impregnation and injection temperatures and pressures are required to make this possible.
  • thermoplastic toughened composites A potential way to efficiently provide thermoplastic toughened composites is to remove the thermoplastic from the resin matrix and apply it in some way directly in or onto the fibres or fabric. This can be achieved using several approaches.
  • hybrid matrix thermosetting resins including a high molecular weight thermoplastic polymer, as a particulate dispersion as disclosed for example in GB-A-2060490 , or as a particulate coating or film interleave of the fibre-reinforced matrix resin prepregs as disclosed in US-A-5057353 .
  • dispersion is typically poor due to difficulty in controlling distribution of particles and uniformity of particle size which can influence rate and degree of melting, and the barrier effect of a continuous film present in the matrix.
  • US 5288547 discloses prepregs for curable compositions comprising thermoplastic polymer membrane interleave which is porous.
  • the membrane is incorporated in the prepreg during preparation, the membrane laid up against a sheet of reinforcing fibre and melting at elevated temperature and pressure to impregnate the fibres; alternatively prepreg is laid up with membrane therebetween and melted to impregnate prior to curing to form a composite part; alternatively the membrane is proposed for RTM application laid up between layers of dry fibre in a mould, melted to impregnate, and liquid resin injected into the mould.
  • thermoplastic and resin matrix preclude the possibility to pre-blend and do not blend or diffuse effectively on curing.
  • polymers such as toughening agents for example thermoplastics.
  • thermoplastic polymer in the form of strong stitching such as polyester to hold complex reinforcing structures together, such as 3-dimensional non-crimped fabrics (NCF), so that fibres are held in place in alignment and orientation during the injection, infusion or application of thermosetting resin.
  • the stitches are of very high melting point polymer such as 230°C, which is moreover orientated and therefore quite crystalline so that melting or solution are not possible, the stitching remains intact post cure.
  • flexible polymer elements may be provided in the form of fibres and the like, which are useful for stitching, which dissolve in the curable composition.
  • compositions may be provided comprising elevated levels of viscous component polymers, by means of providing the viscous polymer in both fluid form and in flexible polymer element solid phase form.
  • a curable composition comprising a polymer element wherein the flexible polymer element is in solid phase and adapted to undergo at least partial phase transition to fluid phase on contact with a resin matrix component of the curable composition in which it is soluble, at a temperature which is less than the temperature for substantial onset of gelling and/or curing of the curable composition.
  • Reference herein to a flexible polymer element is to any shaped element which is both chemically and physically adapted to be at least partially dissolved in a resin matrix making up the curable composition whereby the polymer is dispersed at least partially into the matrix as a common phase by dissolution whereby it loses at least partially its physical element form to the curable composition.
  • the at least one flexible polymer element is elongate in at least one direction for example comprises a textile such as a mono or multi fibre or filament, ribbon, film or mixtures or weave thereof.
  • the flexible polymer element is adapted to dissolve during the preliminary stages of the curing process, during temperature ramping to the temperature for onset of gelling and/or curing, whereby the composition is held in desired configuration by the flexible polymer element until the curable component viscosity increases, obviating the need for support by the flexible polymer element or by a mould.
  • the flexible polymer element may be adapted for use in the presentation or processing of the curable composition whereby the dissolved polymer therefrom may be substantially undetectable and insignificant in the properties of the cured composition. It is a particular advantage that flexible polymer elements may be provided which are soluble and may be traceless in the cured product, yet strong enough for use in supporting, carrying or assembling other composition components. Alternatively the flexible polymer element may be for use as a component of the curable composition and adapted to contribute to the properties of the end product. It is a further advantage that curable compositions may be provided in which viscous polymers may be included making up a significant part of the polymer phase of the end product. Alternatively the flexible polymer element may be for use in the processing of a curable composition with improved composite properties, and may be traceless or otherwise in the final cured product.
  • the fluid phase of the flexible polymer element undergoes excellent dispersion by solvating effect of curable component This is particularly important to the properties of the cured product.
  • scanning by Raman spectroscopy at co-ordinates throughout the cured product shows 100% dispersion, with identical scans at each co-ordinate.
  • flexible polymer elements provide an excellent outlife and remain in solid phase at ambient or elevated temperature, up to 300 or 400°C, in the absence of dissolving resin, and can be left for years at or below this temperature, without advance of the composition, and can thereafter undergo phase transition as desired by contact with dissolving resin and curing under conditions as hereinbefore defined, for example temperatures in excess of 60C, for example of the order of 140°C.
  • Phase transition is by solution, optionally assisted by heat, in a resin matrix component of the curable composition. It is a particular advantage that that soluble polymer elements enable improved blending.
  • the polymer of the flexible element may be adapted to form a common phase on curing of the curable composition, e.g. in solution in the thermosetting resin or may wholly or partially phase separate to produce a two phase matrix resin system.
  • the toughness of the thermoset/thermoplastic blends is related, among other things, to the morphology and phase sizes in the cured blend.
  • the desired level of matrix resin toughness is obtainable by control of the morphology and phase sizes in the thermoset/thermoplastic blend through the chemistries of the thermoplastic polymer and the thermosetting resin precursors, as well as the other parameters of any desired morphology.
  • Figures B1 and B4 illustrate the process of dissolution, and phase separation in the case of a fibre as flexible polymer element characterised by complete dissolution.
  • Figure B4 is shown typical two phase morphologies obtained in thermoplast/thermoset systems, which may be obtained according to the present invention.
  • Phase transition e.g. solution of flexible element may be determined or monitored with use of any suitable techniques, for example TEM, SEM and the like and such techniques may be employed by those skilled in the art to determine suitable flexible element characteristics and curable composition characteristics and processing conditions for commercial production of cured compositions.
  • the polymer forming the flexible polymer element is preferably adapted to undergo phase transition, i.e. to at least partially dissolve in the resin matrix at a temperature Ts in a range at least part of which is less than the cure temperature of the resin matrix Tc.
  • the polymer element may be configured in manner to improve or hinder thermal conductivity and speed or slow transfer of heat into the element to endure rapid or delayed solution thereof.
  • the polymer element may undergo complete or partial phase transition, e.g. may completely dissolve, or may partially dissolve whereby a portion thereof is dispersed into the matrix and a portion retains its elemental form, either by ensuring that precuring time and temperature are insufficient for complete dissolution or preferably by providing the polymer as a blend or co-polymer with one or more further insoluble polymers, for example in the form of a random or block co-polymer or other blend or derivative with organic or inorganic substrates.
  • the polymer element may be combined with one or more further polymers or other soluble or insoluble organic or inorganic substrates in the cured composition.
  • the flexible element may contain for example conventional toughening agents such as liquid rubbers having reactive groups, aggregates such as glass beads, rubber particles and rubber-coated glass beads, metal particles such as Ti, Al or Fe, filler such as polytetrafluorethylene, silica, graphite, boron nitride, clays such as mica, talc and vermiculite, pigments, nucleating agents, and stabilisers such as phosphates; agents for increased solvent resistance such as F-containing agents, flame retardants such as metal oxides FeO & TiO crystalline polymers incorporated as blend or as block or random copolymer for example polyether ketones; conventional binder such as low MW thermoset monomers for example epoxy, acrylic, cyanate, ester, BMI-type polymers and the like; conventional adhesives such as epoxy polymers and the like; conventional coating agents etc.
  • conventional toughening agents such as liquid rubbers having reactive groups, aggregates such as glass beads, rubber particles and rubber-coated glass beads, metal particles such as Ti, Al or
  • particles, beads and the like have size in the nm and micron range, according to the thickness or diameter of the flexible polymer element, preferably clay particles are 0.5 to 5nm e.g. 0.1 nm, Ti particles may be 1-6 micron e.g. 2 micron.
  • the flexible polymer element of the present invention serves as an excellent carrier whereby concerns such as viscosity, incompatible polymer melt temperatures and the like are overcome.
  • the flexible polymer element is in a form suitable for intimate mixing with other component(s) of a curable composition, e.g. in the form of a fibre, filament, ribbon, or the like, and in the case that local distribution is desired the flexible polymer element may be in any of these forms or in any other form suitable for non-intimate presentation in the other component(s), e.g. a film for coating, adhesion or local effect, e.g. toughening reinforcement.
  • the flexible element preferably is a fibre or filament having diameter d, or is a film or ribbon having thickness t wherein d or t are in the range up to 100 micron, preferably from 1 to 80 micron for example 30-80 micron, more preferably 30-65 micron. Flexibility is a compromise between element thickness or diameter and polymer modulus.
  • Fibres may be provided in desired Tex (weight fibre in g/m fibre, indicating the linear density) which may be in the range 5 - 150 Tex, and is controlled in known manner during the fibre preparation.
  • the element is preferably characterised by a % elongation to break in the range 1-75, preferably 3-50% lower for stitching application and higher for weaving application, conferred by polymer type and by the method of manufacture, e.g. stretching and orientation; also by toughness measured as Dtex, the linear density based on element, e.g. fibre weight per unit length.
  • the flexible polymer element is conformable, deformable, drapeable or manipulateable in suitable manner to be presented in a curable composition as hereinbefore defined.
  • physical interactions are created during the manufacture of the polymer element which induce or enhance flexibility to particularly advantageous effect by virtue of orientation, chain interaction, individual polymer chain characteristics and the like, contributing to elastomeric behaviour and properties of stretch and strength, enabling knotting, stitching, winding and the like.
  • the flexible polymer element may be characterised by binding or adhesion properties, for example conferred by softening above ambient temperatures, or comprising monomers for example thermoset (epoxy) monomers or other known binders, to assist in the physical association in a curable composition as hereinbefore defined.
  • the flexible polymer element of the invention is particularly suitable for use in LM technology as hereinbefore defined.
  • the polyaromatic comprises polyether sulphone, more preferably a combination of polyether sulphone and of polyether ether sulphone linked repeating units, in which the phenylene group is meta- or para- and is preferably para and wherein the phenylenes are linked linearly through a single chemical bond or a divalent group other than sulphone, or are fused together.
  • fractional reference is made to the average value for a given polymer chain containing units having various values of n or a.
  • the repeating unit -(PhSO 2 Ph)- is always present in said at least one polyarylsulphone in such a proportion that on average at least two of said units - (PhSO 2 Ph) n are in sequence in each polymer chain present, said at least one polyarylsulphone having reactive pendant and/or end groups.
  • the relative proportions of the said repeating units is such that on average at least two units (PhSO 2 Ph) n are in immediate mutual succession in each polymer chain present and is preferably in the range 1 : 99 to 99 : 1, especially 10 : 90 to 90 : 10, respectively. Typically the ratio is in the range 75 - 50 (Ph) a , balance (PhSO 2 Ph) n .
  • the units are:
  • the preferred relative proportions of the repeating units of the polyarylsulphone may be expressed in terms of the weight percent SO 2 content defined as 100 times (weight of SO 2 )/(weight of average repeat unit).
  • the polyarylsulphone may contain up to 50 especially up to 25% molar of other repeating units: the preferred SO 2 content ranges (if used) then apply to the whole polymer.
  • Such units may be for example of the formula: - Ar - A - Ar - in which A is a direct link, oxygen, sulphur, -CO- or a divalent hydrocarbon radical.
  • the polyarylsulphone When the polyarylsulphone is the product of nucleophilic synthesis, its units may have been derived for example from one or more bisphenols and/or corresponding bisthiols or phenol-thiols selected from hydroquinone, 4,4'dihydroxybiphenyl, resorcinol, dihydroxynaphthalene (2,6 and other isomers), 4,4'-dihydroxybenzophenone, 2,2'di(4-hydroxyphenyl)propane and-methane.
  • one or more bisphenols and/or corresponding bisthiols or phenol-thiols selected from hydroquinone, 4,4'dihydroxybiphenyl, resorcinol, dihydroxynaphthalene (2,6 and other isomers), 4,4'-dihydroxybenzophenone, 2,2'di(4-hydroxyphenyl)propane and-methane.
  • a bis-thiol it may be formed in situ, that is, a dihalide as described for example below may be reacted with an alkali sulphide or polysulphide or thiosulphate.
  • Additional units are of the formula: - Ph - Q (Ar- Q') n - Ph - in which Q and Q', may be the same or different, are CO or SO 2 :
  • Ar is a divalent aromatic radical; and n is 0, 1, 2 or 3 provided that n is not zero where Q is SO 2 .
  • Ar is preferably at least one divalent aromatic radical selected from phenylene, biphenylene or terphenylene.
  • Particular units have the formula: -Ph-Q-[-Ph-)m-Q'-]n-Ph- where m is 1, 2 or 3.
  • such units may have been derived from one or more dihalides, for example selected from 4,4'-dihalobenzophenone, 4,4' bis(4-chlorophenylsulphonyl)biphenyl, 1,4,bis(4-bis(4-halobenzoyl)benzene and 4,4' -bis(4-halobenzoyl)biphenyl.
  • dihalides for example selected from 4,4'-dihalobenzophenone, 4,4' bis(4-chlorophenylsulphonyl)biphenyl, 1,4,bis(4-bis(4-halobenzoyl)benzene and 4,4' -bis(4-halobenzoyl)biphenyl.
  • the polyaromatic polymer may be the product of nucleophilic synthesis from halophenols and/or halothiophenols. In any nucleophilic synthesis the halogen if chlorine or bromine may be activated by the presence of a copper catalyst.
  • any nucleophilic synthesis of the polyaromatic is carried out preferably in the presence of one or more alkali metal salts, such as KOH, NaOH or K2CO3 in up to 10% molar excess over the stoichiometric.
  • the polymer may be characterised by a range of MW which may typically be defined either by Mn, peak MW and other means, usually determined by nmr and gpc.
  • the polymer is selected in the range up to 70,000 for example 9000-60,000 for toughening, and in this case the number average molecular weight Mn of the polyaromatic is suitably in the range 2000 to 25000, preferably 2000 to 20000, more preferably 5000 or 7000 to 18000, most preferably 5000 or 7000 to 15000.
  • the polyaromatic is preferably of relatively low molecular weight. It also preferably contains in-chain, pendant or chain-terminating chemical groups which are capable of self-assembling to form higher molecular weight complexes through non covalent bonds with similar or different chemical groupings in the polymer. These maybe, for example, hydrogen bonds, London forces, charge transfer complexes, ionic links or other physical bonds. Preferably the non-covalent bonds are hydrogen bonds or London forces which will dissociate in solution to regenerate the relatively low molecular weight precursor polyaromatic.
  • the polyaromatic preferably contains pendant or chain-terminating groups that will chemically react with groups in the thermosetting resin composition to form covalent bonds.
  • groups may be obtained by a reaction of monomers or by subsequent conversion of product polymer prior to or subsequently to isolation.
  • groups are of formula: -A'-Y where A' is a divalent hydrocarbon group, preferably aromatic, and Y is a group reactive with epoxide groups or with curing agent or with like groups on other polymer molecules.
  • Y are groups providing active hydrogen especially OH, NH 2 , NHR' or -SH, where R' is a hydrocarbon group containing up to 8 carbon atoms, or providing other crosslinking reactivity especially epoxy, (meth)acrylate, cyanate, isocyanate, acetylene or ethylene, as in vinyl allyl or maleimide, anhydride, oxazaline and monomers containing saturation.
  • Preferred end groups include amine and hydroxyl.
  • the polymer of the flexible polymer element may have low molecular weight, but be adapted to react on curing to provide the higher molecular weight required for effective toughening or the like, as disclosed in co-pending GB 0020620.1 the contents of which are incorporated herein by reference. This is of particular advantage since it further alleviates the problems of high viscosity.
  • the polymer may comprise chains of at least one aromatic polymer or a mixture thereof together with at least one chain linking component wherein the at least one aromatic polymer comprises polymer chains of number average molecular weight (Mn) in a first range of 2000 to 11000, especially 3000 to 9000 and characterised by a polymer flow temperature, and wherein one of the at least one polyaromatic and the at least one chain linking component comprises at least one reactive end group and the other comprises, at least two linking sites reactive end groups Y and chain linking sites, Z are selected OH, NH 2 , NHR or SH wherein R is a hydrocarbon group containing up to 8 carbon atoms, epoxy, (meth)acrylate, (iso)cyanate, isocyanate ester, acetylene or ethylene as in vinyl or allyl, maleimide, anhydride, acid, oxazoline and monomers containing unsaturation characterised in that a plurality of the end groups are adapted to react with the linking sites at chain linking temperature in excess of the polymer
  • Flow temperature is defined as the temperature at which the polymer attains a suitably fluid state to enable a degree of polymer chain mobility to align itself for reaction.
  • the flow temperature corresponds to a solution temperature at which the polyaromatic dissolves.
  • Chain linking temperature is defined as the temperature at which the polymer chain ends reaction is initiated.
  • the chain linking temperature is higher than a product processing temperature, to remove solvent and improve wet out of the prepreg which leads to better quality prepreg with easier handling characteristics.
  • the chain linking temperature corresponds to the gelling or curing temperature.
  • Chain linking components are preferably selected from the formula B(Z)n
  • the reactive end group is hydroxy and corresponds to a linking site functionality which is epoxy, whereby reaction thereof produces a ⁇ hydroxy ether linkage in polymers of increased number average molecular weight having either hydroxy or epoxy end groups as desired.
  • the reactive end group is NH 2 and the linking site functionality is anhydride, whereby reaction thereof produces an imide linkage in polymers of increased number average molecular weight having NH 2 or anhydride end groups.
  • the reactive end group is NH 2 and the linking site functionality is maleimide. Mixtures of the above may be employed to produce a mixed architecture including a plurality of reactive end group-linking site combinations.
  • Preferred linking components include multifunctional .epoxy resins, amines and in particular triazines, and anhydrides.
  • Suitable epoxy resins and amines are selected from resins hereinafter defined for matrix resins, and are preferably selected from MY0510, Epikote 828 [O(CH 2 CH)CH 2 0 Ph] 2 C(CH 3 ) 2 and the Cymel class of epoxies including Cymel 0510, benzophenone tetra carboxylicacid dianhydride (BTDA)[O(CO) 2 Ph]zCO, and maleic anhydride.
  • BTDA benzophenone tetra carboxylicacid dianhydride
  • Preferably flexible elements comprising two or more polymers comprise a blend or copolymer of amorphous polymers or of amorphous and semi crystalline polymer. This is of particular advantage in enabling the preparation of multiblock compositions having lowered processing temperatures whilst nevertheless retaining excellent product properties such as solventresistance.
  • the flexible polymer element as hereinbefore defined can be prepared by known or novel methods, for example comprising track etching or mechanical stretching the polymer resin melt, phase precipitation methods such as immersion, evaporation, solvent casting, thermal and humidity methods or forming the element from its monomeric precursor and polymerising.
  • elements in the form of fibres or film are obtained by continuous extrusion of resin melt onto reels and film forming or spinning as known in the art of synthetic textiles manufacture by mechanical stretching with heating, more preferably by providing the polymer melt, drawing off in elemental shape, subjecting to a heating and mechanical stretching regime which may orient polymer chains and render the element elastomeric and predisposed to dissolution, and cooling, preferably by pulling in air for a desired distance, eg 50 to 500mm.
  • polymer melt is drawn off through a die head or the like providing a desired number of apertures or slots, using a pump with controlled pump rate for a desired linear density (Tex) of polymer for example up to 180 Tex.
  • Tex linear density
  • the element may be prepared from micronised or unmicronised polymer, pellets or other extrudate and the like.
  • Preferably fibres are prepared as multifilaments of up to 20 same or different polymer filaments, which are drawn off from the molten polymer, cooled and optionally twisted as desired, and then subjected to heating and stretching.
  • the multifilament is more resistant to breaking, there is a trade off between higher strength and lower flexibility in selection of filaments and twists/metre. Twisting is conventionally used for preparing stitching fibres, to counteract undesired natural twist and breakage.
  • a support structure or carrier for a curable composition comprising at least one flexible polymer element as hereinbefore optionally defined together with structural elements, preferably reinforcing fibres, wherein the at least one flexible polymer element is present in solid phase and adapted to undergo at least partial phase transition to fluid phase on contact with a resin matrix component of a curable composition in which the element is soluble, at a temperature which is less than the temperature for substantial onset of gelling and/or curing of the curable component.
  • Reference herein to a support structure or carrier is to a presentation of the polymer element in physical, preferably intimate association with the reinforcing fibres, for example mono or multi filament fibres, ribbons and/or films are presented as the fibres or ribbons alone or with reinforcing fibres in a support structure or carrier comprising a fabric, web, weave, non woven, overwinding, preform, scrim, mesh, fleece, roving, prepreg, composite or laminar film or interleave or the like or a mixture thereof, or stitched, sewn, threaded or the like presentations thereof.
  • the polymer element serves to support the further component(s) of the structure or to carry the reinforcing fibres and/or resin matrix, and optionally any further component(s) of a desired curable composition.
  • the support structure or carrier may be mutually supporting or carrying whereby the at least one flexible polymer element is additionally supported by or carried by the reinforcing fibres or an additional resin matrix.
  • references herein to structural or reinforcing fibres is to insoluble fibres as known in the art which stiffen composites, such as organic or inorganic polymer, carbon, glass, inorganic oxide, carbide, ceramic or metal and the like fibres.
  • the support structure or carrier of the invention may have any number of physical presentations.
  • the support structure or carrier may be in the form of a preform as known in the art but wherein the flexible polymer element is present as fibres or ribbons amongst the reinforcing fibres in aligned or mis-aligned or stitched fashion or as a multi filament of soluble polymers fibres and reinforcing fibres which may be braided, spun or over wound, or is present as a film laid up against the reinforcing fibres and adhered or crimped or otherwise physically associated therewith.
  • Particularly advantageous presentations include non-crimped fabrics of reinforcing fibre with flexible polymer fibre stitching, preforms of aligned or random reinforcing and flexible polymer fibres which may be stitched or punched or softened to confer binding, or other configurations in which flexible polymer element is presented non uniformly with respect to the reinforcing fibre, to locally confer properties such as toughening and the like characteristic of the flexible polymer, for example around bolt holes, fastening apertures, high stress panels and the like.
  • the at least one flexible element is a monofilament or low twist/metre higher multifilament fibre, optionally cut to comparable length and simply admixed.
  • the element is monofilament or lower multifilament.
  • the structure or carrier can be formed at any suitable stage in the manufacture of the fabric based reinforcements. It can also be applied after the manufacture of the fabric for example in the case where a hole is created in the assembled fabrics (preforms) or to physically stitch multi-component parts together, prior to resin injection/infusion.
  • a support structure or carrier as hereinbefore defined preferably comprises structural fibres, laid up in desired manner, and fibre form flexible polymer element in the form of stitching, adapted to undergo phase transition as hereinbefore defined in manner to disperse locally or universally in the curable composition.
  • the support structure or carrier comprises therefore a fabric in which the structural fibres or fabric are laid up in random, mono or multiaxial, (co) linear or (co) planar arrangement and the flexible polymer element fibres are in the form of stitching in conventional manner securing the fibre or fabric or assemblies thereof as desired.
  • stitching comprises upper and lower thread securing fibres, fabrics or assemblies thereof from opposite faces.
  • the support structure or carrier provides at least partially traceless stitching, preferably provides traceless stitching.
  • the invention provides a support structure or carrier comprising the above mentioned lay up and stitching, specifically the invention provides traceless stitching.
  • a process for the preparation of a support structure or carrier as hereinbefore defined comprising providing at least one flexible polymer element, and providing reinforcing fibres as hereinbefore defined and combining in manner to provide a physical association thereof.
  • Combining to provide a physical intimate association may be by methods as known in the art of textiles, for example by stitching, knitting, crimping, punching, (uni)weaving, braiding, overwinding, (inter) meshing, comingling, aligning, twisting, coiling, knotting, threading and the like.
  • a support structure or carrier may be prepared in continuous manner for example as a roll of fabric which may be tailored by stitching and weaving in desired manner, for example cross stitching to prevent fabric distortion on handling, provide folding seams, directional strengthening and the like.
  • Structural fibres as hereinbefore defined can be short or chopped typically of mean fibre length not more than 2cm, for example about 6mm.
  • the fibres are continuous and may, for example, be unidirectionally-disposed fibres or a woven fabric, i.e. the composite material comprises a prepreg. Combinations of both short and/or chopped fibres and continuous fibres may be utilised.
  • the fibres may be sized or unsized.
  • Reinforcing fibres can be added typically at a concentration of 5 to 35, preferably at least 20% by weight.
  • continuous fibre for example glass or carbon, especially at 30 to 70, more especially 50 to 70% by volume.
  • the fibre can be organic, especially of stiff polymers such as poly paraphenylene terephthalamide, or inorganic.
  • glass fibres such as "E” or “S” can be used, or alumina, zirconia, silicon carbide, other compound ceramics or metals.
  • a very suitable reinforcing fibre is carbon, especially as graphite.
  • Graphite fibres which have been found to be especially useful in the invention are those supplied by Amoco under the trade designations T650-35, T650-42 and T300; those supplied by Toray under the trade designation T800-HB; and those supplied by Hercules under the trade designations AS4, AU4, IM 8 and IM 7, and HTA and HTS fibres.
  • Organic or carbon fibre is preferably unsized or is sized with a material that is compatible with the composition according to the invention, in the sense of being soluble in the liquid precursor composition without adverse reaction or of bonding both to the fibre and to the thermoset/thermoplastic composition according to the invention.
  • a material that is compatible with the composition according to the invention in the sense of being soluble in the liquid precursor composition without adverse reaction or of bonding both to the fibre and to the thermoset/thermoplastic composition according to the invention.
  • carbon or graphite fibres that are unsized or are sized with epoxy resin precursor.
  • Inorganic fibre preferably is sized with a material that bonds both to the fibre and to the polymer composition; examples are the organo-silane coupling agents applied to glass fibre.
  • a curable composition comprising a flexible polymer element or a support structure or carrier as hereinbefore defined and curable resin matrix, together with optional additional reinforcing fibres, and catalysts, curing agents, additives such as fillers and the like.
  • a matrix resin is selected from the group consisting of an epoxy resin, an addition-polymerisation resin, especially a bis-maleimide resin, a formaldehyde condensate resin, especially a formaldehyde-phenol resin, a cyanate resin, an isocyanate resin, a phenolic resin and mixtures of two or more thereof, and is preferably an epoxy resin derived from the mono or poly-glycidyl derivative of one or more of the group of compounds consisting of aromatic diamines, aromatic monoprimary amines, aminophenols, polyhydric phenols, polyhydric alcohols, polycarboxylic acids, cyanate ester resin, benzimidazole, polystyryl pyridine, polyimide or phenolic resin and the like, or mixtures thereof.
  • addition-polymerisation resin are acrylics, vinyls, bis-maleimides, and unsaturated polyesters.
  • formaldehyde condensate resins are urea, melamine and phenols.
  • thermosetting matrix resin comprises at least one epoxy, cyanate ester or phenolic resin precursor, which is liquid at ambient temperature for example as disclosed in EP-A-0311349 , EP-A-0365168 , EP-A-91310167.1 or in PCT/GB95/0I303 .
  • thermoset is an epoxy or cyanate ester resin or a mixture thereof.
  • An epoxy resin may be selected from N,N,N'N'-tetraglycidyl diamino diphenylmethane (e.g. "MY 9663", “MY 720” or “MY 721” sold by Ciba-Geigy) viscosity 10 - 20 Pa s at 50°C; (MY 721 is a lower viscosity version of MY 720 and is designed for higher use temperatures); N,N,N',N-tetraglycidyl-bis(4-aminophenyl)-1,4-diiso-propylbenzene (e.g.
  • Epon 1071 sold by Shell Chemical Co. viscosity 18 - 22 Poise at 110°C
  • triglycidyl ethers of p-aminophenol e.g.
  • DEN 431 or “DEN 438” sold by Dow), varieties in the low viscosity class of which are preferred in making compositions according to the invention
  • diglycidyl 1,2-phthalate e.g. GLY CEL A-100
  • diglycidyl derivative of dihydroxy diphenyl methane e.g. "PY 306” sold by Ciba Geigy
  • Other epoxy resin precursors include cycloaliphatics such as 3',4'-epoxycyclohexyl-3,-4-epoxycyclohexane carboxylate (e.g. "CY 179" sold by Ciba Geigy) and those in the "Bakelite” range of Union Carbide Corporation.
  • the Y is a linking unit selected from the group consisting of oxygen, carbonyl, sulphur, sulphur oxides, chemical bond, aromatic linked in ortho, meta and/or para positions and/or CR 2 wherein R 1 and R 2 are hydrogen, halogenated alkanes, such as the fluorinated alkanes and/or substituted aromatics and/or hydrocarbon units wherein said hydrocarbon units are singularly or multiply linked and consist of up to 20 carbon atoms for each R 1 and/or R 2 and P(R 3 R 4 R' 4 R 5 ) wherein R 3 is alkyl, aryl alkoxy or hydroxy, R' 4 may be equal to R 4 and a singly linked oxygen or chemical bond and R 5 is doubly linked oxygen or chemical bond or Si(R 3 R 4 R' 4 R 6 ) wherein R 3 and R 4 , R' 4 are defined as in P(R 3 R 4 R' 4 R 5 ) above and R 5 is defined similar to R 3 above.
  • cyanate esters include cyanate esters of phenol/formaldehyde derived Novolaks or dicyclopentadiene derivatives thereof, an example of which is XU71787 sold by the Dow Chemical Company, and low viscosity cyanate esters such as L10 (Lonza, Ciba-Geigy, Bisphenol derived).
  • a phenolic resin may be selected from any aldehyde condensate resins derived from aldehydes such as methanal, ethanal, benzaldehyde or furfuraldehyde and phenols such as phenol, cresols, dihydric phenols, chlorphenols and C 1-9 alkyl phenols, such as phenol, 3- and 4- cresol (1-methyl, 3- and 4- hydroxy benzene), catechol (2- hydroxy phenol), resorcinol (1, 3- dihydroxy benzene) and quinol (1, 4- dihydroxy benzene).
  • phenolic resins comprise cresol and novolak phenols.
  • Suitable bismaleimide resins are heat-curable resins containing the maleimido group as the reactive functionality.
  • the term bismaleimide as used herein includes mono-, bis-, tris-, tetrakis-, and higher functional maleimides and their mixtures as well, unless otherwise noted. Bismaleimide resins with an average functionality of about two are preferred.
  • Bismaleimide resins as thus defined are prepared by the reaction of maleic anhydride or a substituted maleic anhydride such as methylmaleic anhydride, with an aromatic or aliphatic di- or polyamine. Examples of the synthesis may be found, for example in U.S. Patent Nos.
  • nadicimide resins prepared analogously from a di- or polyamine but wherein the maleic anhydride is substituted by a Diels-Alder reaction product of maleic anhydride or a substituted maleic anhydride with a diene such as cyclopentadiene, are also useful.
  • bismaleimide shall include the nadicimide resins.
  • Preferred di- or polyamine precursors include aliphatic and aromatic diamines.
  • the aliphatic diamines may be straight chain, branched, or cyclic, and may contain heteroatoms. Many examples of such aliphatic diamines may be found in the above cited references.
  • Especially preferred aliphatic diamines are hexanediamine, octanediamine, decanediamine, dodecanediamine, and trimethylhexanediamine.
  • the aromatic diamines may be mononuclear or polynuclear, and may contain fused ring systems as well.
  • Preferred aromatic diamines are the phenylenediamines; the toluenediamines; the various methylenedianilines, particularly 4,4'-methylenedianiline; the naphthalenediamines; the various amino-terminated polyarylene oligomers corresponding to or analogues to the formula H 2 N-Ar[X-Ar] n NH 2 , wherein each Ar may individually be a mono- or poly-nuclear arylene radical, each X may individually be -0-, -S-, -C0 2 , -S0 2 -, -0-C0-, C 1 -C 10 lower alkyl, C 1 -C 10 halogenated alkyl, C 2 -C 10 lower alkyleneoxy, aryleneoxy, polyoxyalkylene or polyoxyarylene, and wherein n is an integer of from about
  • bismaleimide "eutectic" resin mixtures containing several bismaleimides. Such mixtures generally have melting points which are considerably lower than the individual bismaleimides. Examples of such mixtures may be found in U.S. Patent Nos. 4,413,107 and 4,377,657 . Several such eutectic mixtures are commercially available.
  • the flexible polymer element and dissolving matrix are selected as a "solution pair" providing not only dissolution at desired time and temperature, but also good matrix injection, dispersion, morphology such as phase separation and traceless dispersion if desired, and the like.
  • Suitable solution pairs include a low viscosity matrix resin for good injection and rapid dissolution, and compatibility of matrix rein and element resin. Alternatively or additionally less compatible resins may be used if it is desired to introduce phase separation for enhanced mechanical properties. Combinations of different viscosity resins may be used each contributing various of the above properties where these are not provided by a single resin.
  • the flexible polymer element may be present as fibres in the form of a prepreg with the matrix resin in known manner, as a film in the form of an interleave with matrix film or as a porous or foamed film impregnated with matrix resin or the like.
  • the present invention is of particular advantage in the case that the flexible polymer element comprises in fluid phase a highly viscous polymer or a precursor thereof.
  • the curable composition preferably comprises at least one curable thermoset matrix resin_as hereinbefore defined and optionally at least one thermoplast matrix resin.
  • compositions confer enhanced beneficial properties in the end product, whereby composites may be provided to higher specification.
  • this may be achieved simply by incorporating additives or by increasing the quantity of a component.
  • it has proved problematic to increase the quantity of high viscosity resins beyond a limiting amount at which it is no longer possible to achieve a high quality blend with the additional composition components, and many properties of such resins cannot be conferred by other materials or additives. This is particularly the case with viscous thermoplastic resins, in preparing high strength low weight engineering materials.
  • the curable composition provides elevated levels of thermoplast polymer whereby the thermoplastic resin is present in a first amount in fluid phase as a matrix component and additionally is present in a second amount in the form of at least one flexible polymer element in solid phase.
  • thermoplastic resin component comprises at least one thermoplastic polymer and may be a blend of thermoplastic polymers in first or second amounts or the same or different thermoplastic polymer in first and second amount.
  • the thermoplastic resin component may be present in any suitable amounts.
  • the thermoplastic resin component is present in first fluid phase amount of from 1 wt % up to that amount which it is possible to blend with the matrix resin and/or impregnate into the reinforcing fibres, preferably from 1 wt % to 15 wt %, more preferably from 5 wt % to 12.5 wt %; and is present in second solid phase amount of from 1 wt% up to any desired amount which is suitable for the desired purpose, preferably from 1 wt % to 50 wt %, more preferably from 5 wt % to 30 wt %, most preferably from 5 wt % to 20 wt %.
  • the composition of the invention may comprise the thermoplastic resin component in a total amount of from 2 wt % to 65wt % of the composition.
  • thermoplastic resin component or the like in a composition by providing a part thereof in the form of a flexible polymer element such as a fibre, film or the like which is capable of dissolving in a resin matrix, whereby it may be uniformly and controllably combined in a curable composition and uniformly dispersed by means of at least partial phase transition as herein before defined to provide a polymer blend having desired properties.
  • thermosetting resin matrix capable of undergoing phase transition in a thermosetting resin matrix
  • thermoplast-containing resin matrix specifically a thermoplast-thermoset resin matrix
  • composites comprising elevated levels of a thermoplast resin component obtained in this manner exhibit enhanced properties as a result of the elevated thermoplast content.
  • a curing agent is suitably selected from any known thermoset curing agents, for example epoxy curing agents, as disclosed in EP-A-0 311 349 , EPA 91310167.1 , EP-A-0 365 168 or in PCT/GB95/01303 , which are incorporated herein by reference, such as an amino compound having a molecular weight up to 500 per amino group, for example an aromatic amine or a guanidine derivative.
  • thermoset curing agents for example epoxy curing agents, as disclosed in EP-A-0 311 349 , EPA 91310167.1 , EP-A-0 365 168 or in PCT/GB95/01303 , which are incorporated herein by reference, such as an amino compound having a molecular weight up to 500 per amino group, for example an aromatic amine or a guanidine derivative.
  • Particular examples are 3,3'- and 4-,4'-diaminodiphenylsulphone, (available as "DDS” from commercial sources), methylenedianiline,bis(4-amino-3,5-dimethylphenyl)-1,4 diisopropylbenzene (available as EPON 1062 from Shell Chemical Co); bis(4-aminophenyl)-1,4-diisopropylbenzene (available as EPON 1061 from Shell Chemical Co); 4-chlorophenyl-N,N-dimethyl-urea, eg Monuron; 3,4-dichlorophenyl-N,N-dimethyl-urea, eg Diuron and dicyanodiamide (available as "Amicure CG 1200 from Pacific Anchor Chemical).
  • ком ⁇ онент such as aliphatic diamines, amides, carboxylic acid anhydrides, carboxylic acids and phenols can be used if desired. If a novolak phenolic resin is used as the main thermoset component a formaldehyde generator such as hexamethylenetetraamine (HMT) is typically used as a curing agent.
  • HMT hexamethylenetetraamine
  • the flexible polymer element comprises a polyaromatic polymer and the curable composition additionally comprises a catalyst for the polyaromatic polymer.
  • the curing catalyst employed preferably comprises a Lewis acid having amine functionality, instead of in addition to conventional catalysts, as described in copending GB 0002145.1 , the contents of which are incorporated herein by reference.
  • the catalyst is of the formula: LXn.R Where LXn is a Lewis acid and R is an amine.
  • L is selected from Groups IIb, IIIb, VIII of the Periodic Table of the Elements and X is halo.
  • Preferred catalysts include BF 3 , AlF 3 , FeF 3 , ZnF 2 as Lewis acid component and primary or secondary aliphatic or aromatic amine such as monoethyl amine (mea), dimethylamine (dma), benzylamine (bea) or piperidine.
  • a process for the preparation of a curable composition as hereinbefore defined as known in the art comprising contacting a flexible polymer element or a support structure or carrier as hereinbefore defined with resin matrix for example by interleaving impregnating, injecting or infusing, mixing and the like.
  • composition may then be laid up with other component parts such as reinforcing fibres to provide the curable composition, or other composite parts such as metal or polymer or other bodies or structures prior to curing in known manner.
  • component parts such as reinforcing fibres to provide the curable composition, or other composite parts such as metal or polymer or other bodies or structures prior to curing in known manner.
  • Curable compositions of this present invention find utility in producing fabrics which can be composed of a combination of the polymer derived from the flexible polymer element with other resin matrix polymers, such as high molecular weight polyesters, polyamides, e.g. nylons, etc. which are used to form 'scrims' typical of the composite industry.
  • resin matrix polymers such as high molecular weight polyesters, polyamides, e.g. nylons, etc.
  • These 'scrims' are not complete films but possess open weave structures and as such can be used to act as carriers for adhesive resin components.
  • the combination of 'scrim' and resin components are then referred to as adhesive films. Such films can be used to bond composite structures together as well as composite to metallic structures.
  • the flexible polymer element such as soluble fibres, as part of the 'scrim' will dissolve as the adhesive cures and then phase separate to produce the predetermined morphology of choice. This will improve the adhesion properties of the resin to the substrate surfaces as well as increase the cohesive properties of the resin. Appropriate choice of the flexible polymer element may also lead to improvements in environmental resistance of the adhesive bond.
  • thermoplastics into the interlaminar region of conventional prepregs.
  • the scrims can also be utilised in dry preforms where the open weave structure allows the injection/infusion of the thermosetting resins to occur throughout the preform. This is unlike the inclusion of continuous films which act as obstructions to the resin flow which in turn can lead to porosity and poor mechanical and environmental performance.
  • the present invention also finds utility in the area of moulding materials in which the flexible polymer element(s) can be added to a moulding compound formulation in the form of chopped fibres.
  • the fibres are designed to remain intact, i.e. insoluble as the moulding compound travels through an injection moulding machine. This means that the viscosity of the moulding compound will in general be lower and will require lower temperatures and pressures in order to process the moulding resin. It can also mean that other additives, such as fillers and flame retardants can be added to the resin without too detrimental effect upon the moulding compound's viscosity.
  • Soluble fibres can be in a continuous or discontinuous form and admixed with a range of thermoset resins in order to disperse the fibres.
  • Such film products can then be used and applied to the surface or between layers of the main structural reinforcement.
  • Another utility for this invention is in production of continuous films of pure polymer which can either be used as made or further modified to suit a particular application.
  • the soluble fibres and any reinforcing fibres used in the invention are incorporated with the resin matrix at any suitable stage in the process.
  • a curable composition comprising matrix resin optionally containing some volatile solvent can be contacted with the flexible element by a variety of techniques, including impregnation, injection, infusion and the like.
  • a flexible polymer film may be foamed by solvent flashing, with subsequent impregnation to form a composite film, for example carrying an adhesive resin, or multilaminar films may be provided using known techniques.
  • Injection may be at ambient or elevated temperature less than the dissolution temperature as known in the art, suitably in the range room temperature to 100C, preferably room temperature to 75C to confer suitable resin viscosity. Injection may be in known prepreg or preform manner with use of a bag, mandrel and/or mould and optionally with use of channels or the like to assist flow as known in the art. Injection times are suitably in the range 2 to 300 minutes, preferably 2 to 120 minutes for example 2 to 30 minutes.
  • a fibre-reinforced composition is made by passing essentially continuous fibre into contact with such resin composition.
  • the resulting impregnated fibrous reinforcing agent may be used alone or together with other materials, for example a further quantity of the same or a different polymer or resin precursor or mixture, to form a shaped article. This technique is described in more detail in EP-A-56703 , 102158 and 102159 .
  • a further procedure comprises forming incompletely cured matrix resin composition into film by for example compression moulding, extrusion, melt-casting or belt-casting, laminating such films to fibrous reinforcing agent and thermoplastic fibres in the form of for example a non-woven mat of relatively short fibres, a woven cloth or essentially continuous fibre in conditions of temperature and pressure sufficient to cause the mixture to flow and impregnate the fibres and curing the resulting laminate.
  • Plies of impregnated fibrous reinforcing agent especially as made by the procedure of one or more of EP-A 56703 , 102158 , 102159 which additionally contain thermoplastic fibres can be laminated together by heat and pressure, for example by autoclave, vacuum or compression moulding or by heated rollers, at a temperature above the curing temperature of the thermosetting resin or, if curing has already taken place, above the glass transition temperature of the mixture, conveniently at least 180°C and typically up to 200°C, and at a pressure in particular in excess of 1 bar, preferably in the range of 1 - 10 bar.
  • the resulting multi-ply laminate may be anisotropic in which the fibres are continuous and unidirectional, orientated essentially parallel to one another, or quasi-isotropic in each ply of which the fibres are orientated at an angle, conveniently 45° as in most quasi-isotropic laminates but possibly for example 30° or 60° or 90° or intermediately, to those in the plies above and below. Orientations intermediate between anisotropic and quasi-isotropic, and combination laminates, may be used. Suitable laminates contain at least 4 preferably at least 8, plies. The number of plies is dependent on the application for the laminate, for example the strength required, and laminates containing 32 or even more, for example several hundred, plies may be desirable. Woven fibres are an example of quasi-isotropic or intermediate between anisotropic and quasi-isotropic.
  • the laminate may be single or multiply, and include directional strengthening with one or more over laid strengthening fibres, stitched in place with the soluble fibre (TFP).
  • Laminates may be assembled in shaped manner, for example 2 fabrics may be oriented at right angles to each other to form struts and the like, and stitched in place with soluble fibre.
  • a curable composition provided according to the invention is a liquid moulded composition obtained by a liquid moulding method as known in the art wherein a flexible polymer element or a support structure or carrier as hereinbefore defined comprising reinforcing fibres (dry) and the at least one flexible polymer element is placed into a bag, mould or tool to provide a preform and matrix resin is injected/infused directly into the combined fibres and element.
  • a method for the curing of a curable composition comprising providing the composition as hereinbefore defined, providing additional components including other reinforcing matrix components, additives and the like, subjecting to elevated temperature for a period suitable for phase transition of flexible polymer element, and subjecting to further elevated temperature for a period suitable for gelling and/or curing of curable component, and the curing thereof to provide a cured composite.
  • Additional fibre reinforcement or resin matrix may be incorporated with the support structure prior to curing thereof.
  • the preform is preferably formed, injected/infused and cured by processing techniques such as Resin Transfer Moulding (RTM), Liquid Resin Infusion (LRI), Resin Infusion Flexible Tooling (RIFT), Vacuum Assisted Resin Transfer Moulding (VARTM), Resin Film Infusion (RFI) and the like as hereinbefore referred.
  • RTM Resin Transfer Moulding
  • LRI Liquid Resin Infusion
  • RIFT Resin Infusion Flexible Tooling
  • VARTM Vacuum Assisted Resin Transfer Moulding
  • RFI Resin Film Infusion
  • the process includes a preliminary stage of infusion of additional resin matrix at reduced pressure, followed by a degassing stage drawing off air for reducing voidage.
  • the degassing is carried out under elevated pressure.
  • degassing may be carried out at ambient or reduced pressure without void formation with use of a particular support structure or carrier configuration as hereinbefore defined wherein fibres of two different diameters are laid up in coaligned arrangement creating channels therebetween, which assists air flow.
  • the panel may be infused, degassed and cured using RIFT or VARTM techniques such as vacuum bagging, without the need for an external pressure from an autoclave to apply to the bag surface.
  • the support structure or carrier comprises aligned soluble, and optionally additionally structural, fibres of two distinct average diameters.
  • the support structure or carrier comprises therefore a multiaxial fabric in which fibres of a first diameter which may be soluble or structural, are laid up in colinear arrangement with fibres of greater diameter, coaligned along the first fibres, thereby creating longitudinal channels throughout the composition.
  • the first fibres are usually structural fibres, but optionally the embodiment of this invention comprises a support structure or carrier having soluble fibres of two diameters, whereby channels are created therebetween, some or all fibres dissolving on curing to give a composite or neat resin panel of 0% voidage.
  • the fibre form flexible polymer elements remain in fibre form in the initial stages of degassing, at ambient or reduced pressure and draw air off from the panel whereafter the fibres dissolve and disperse without trace allowing the fluid phase components to compact, without external applied pressure, prior to onset of gelling and curing. If external pressure is applied the performance is simply enhanced, however it is a particular advantage that this configuration allows for the first time curing large panels without the need for an autoclave or the like.
  • soluble fibres are present in an amount of 2 to 50 wt%, preferably 2 to 40 wt%, more preferably 4 to 16 wt% in this embodiment.
  • the soluble fibre is present as multifilament of Tex 30 - 160, laid up against structural fibre of diameter 5 to 10 micron eg 6 or 7 micron.
  • the process of the invention comprises subjecting to elevated temperature in the range up to 300°C for example 60 to 200C, more preferably 75 to 150C for a period of up to 45 minutes, preferably 0.5 to 35 minutes to effect phase transition.
  • Temperatures in the range 100-150°C are particularly suitable for phase transition of readily soluble flexible polymer elements for example of low MW, present in readily soluble concentration in an effective curable component solvent, and in the range 150°C to 300°C for less readily soluble flexible polymer elements.
  • Suitable elevated temperature is selected in a desired range to effect phase transition in a desired time, for example a given flexible polymer element may be subjected to elevated temperature in the range 135 to 170°C for 2-10 minutes, 125 to 135°C for 5-30 minutes or 105 to 125°C for 10-40 minutes.
  • Phase transition may be at ambient or elevated pressure corresponding to the desired injection, degassing and curing conditions.
  • the process includes subjecting to further elevated temperature after phase transition to cause onset of gelling or curing.
  • Gelling may be at temperature in the range corresponding to pre cure in known manner. Gelling is preferably followed by further elevated temperature cure, or the gelled composition may be cooled for later curing, for example if gel or cure is in an autoclave, or mould, the composition may be removed from the autoclave or mould and cure continued at ambient pressure in regular oven.
  • Gelling or curing is suitably carried out by known means as elevated temperature and pressure for a suitable period, including temperature ramping and hold as desired.
  • a suitable gelling or cure cycle corresponds to that for a conventional composition comprising the same component types and amounts and reference is made to the description and example illustrating calculation of amount of flexible polymer element present in the composition.
  • Preferably cure is at temperature in the range 180 to 400°C for 1-4 hours, for example. Additionally the process may include post curing at suitable conditions to enhance properties such as Tg and the like.
  • Gelling or curing may be with use of catalysts as hereinbefore defined, whereby temperature increase causes activation, and cooling below activation temperature halts curing.
  • the process may be monitored in real time but preferably a suitable reaction time and temperature is predetermined for a given composition, for example by preparing samples and analysing solution and dispersion after completion of gelling or cure, for example by use of Raman spectroscopy or the like.
  • kit of parts comprising a flexible polymer element as hereinbefore defined, a solution pair resin matrix suitable for dissolving the flexible element, and optional reinforcing fibre as a support structure or carrier or as separate components, together with any additional reinforcing fibres, matrix, monomers or polymers, curing agents and the like.
  • a cured composite or resin body comprising cured matrix resin and optional structural fibres, and dispersed cured polymer derived from soluble flexible polymer elements as hereinbefore defined, in common phase or phase separated from the matrix resin.
  • a method for selecting or blending a resin matrix suitable for assisting in dissolving a flexible polymer element as hereinbefore defined, with reference to class, molecular type, and the like is provided.
  • a complex shaped structure prepared without use of a mould, comprising assembled sections in which flexible polymer element is used as hereinbefore defined as woven and/or stitching to confer mechanical properties and/or to confer planarity, fold seams, reinforcing for hinges and bolt holes, directional strengthening and the like and for assembly, and sections are assembled with use of flexible polymer element as stitching to hold the structure in place during resin injection.
  • Particular structures which may be provided include net shape preforms and assembled panels for use in aerospace, automotive, marine, wind energy and like applications.
  • a flexible polymer element, support structure or carrier, prepreg or preform, curable composition or cured composite or resin body as hereinbefore defined for use in the preparation of an engineering composite, in aerospace, automotive, marine, wind energy, industrial application, in sporting goods and papermills, as an adhesive, functional or protective coating for example for rollers, sheet metal, electrical insulation and the like, in particular as stitched fabric for example in constructing automotive body parts, reinforced films such as monofilm, for reinforcing or filament overwinding in preparation of pipes, tanks, rollers or in reinforcing engineering structures such as bridges and the like.
  • Section A Soluble fibres for a support structure or carrier
  • Polymers are commercially available or may be prepared as described in BP 311349 , WO 99/43731 , GB 000 2145.1 or GB 0020620.1 the contents of which are incorporated herein by reference.
  • fibres are produced both in the laboratory and also on a commercial extruder.
  • Example A2 Spinning of the polymers into fibres using a laboratory scale extruder
  • Example A3 Spinning of the polymers into fibres using an industrial scale extruder.
  • the screw speed was 230 rpm and the T melt of the polymer was 294C.
  • the extruded polymer was water cooled at RT and dragged into a chopper.
  • the average diameter of the pellets was 3 mm.
  • the temperature of the melt polymer was 295C.
  • Pump speed was set to give a desired Tex and desired tenacity at break.
  • Four different Tex fibres of the invention in the range 30 to 60 Tex were obtained with different pump speeds.
  • the minimum screw speed was set at 11 rpm and the following machine parameters were chosen to give a mono filaments fibre diameter of 30 microns: Spinning die head diameter x holes 0.3mm x 100 Quench bath temperature 60C 1 st Stretching unit speed Not used 1st orientation oven temperature 25C 2 nd stretching unit speed 200m/min 2 nd orientation oven temperature 25C 3 rd stretching unit speed 200m/min 3 rd oven temperature 25C 4 th stretching unit speed 200m/min
  • Fibres were pulled in air for a distance of 50 to 500mm, according to desired modulus.
  • the polymers detailed in Table 1 were all evaluated in this temperature range and an optimum melt temperature was selected that gave the best quality fibre from both hot melt extrusion and the melt flow indicator.
  • the optimum melt temperature for the series of 40:60 PES:PEES copolymers was different to that for the 100% PES, for which a higher minimum melt temperature was required, and higher temperatures were required in order to reduce melt strength and be able to draw thin fibres.
  • Flexible polymer elements or support structures or carriers of the invention can therefore be stored at ambient or elevated temperature for extended periods up to years without dissolution, and only on contacting with solvent does the element dissolve in the order of minutes up to days.
  • Flexibility is empirical and is inversely proportional to diameter, and is a function of modulus
  • flexible elements may be selected by polymer type to provide desired properties for stitching, weaving, comingling or other desired support or carrier function, with reference to their inherent properties.
  • PES and TRIVERA are both typical examples of commercial multi-filament polyester stitch used to stitch carbon fibre fabrics. It should be noted that all other fibres studied are examples of single mono filament fibres.
  • Section B Support structure or carrier comprising soluble fibre and dissolving matrix resin
  • Figure B1 shows figuratively the dissolution process, derived from photographic images.
  • Figures B1a and B1b show time temperature curves for dissolution of fibres in epoxy resin, for different formulations, and also showing the time to dissolution and time to gel at different temperatures, indicating that very fine control of solution and of gelling onset can be provided by the present invention ensuring complete fibre dissolution before onset of gelling.
  • Example B2 Dispersion of soluble fibre in matrix resin and mechanical testing
  • Figure B2a shows the preparation of panels for mechanical testing and diffusion studies through Raman.
  • Figures B2b to B2d show Raman spectra of the cured composite. The microscope was focussed at different points on the resin block, several nm apart, just below the surface.
  • Tests were conducted on several panels prepared with different level of soluble fibres.
  • Figure B3a and b show energy and strength fracture toughness, the results are almost identical, in each case the system with soluble fibres showing higher Gc and Kc at thermoplastic content ⁇ 10% and > 17%.
  • Polysulphone fibre was dissolved in L10 cyanate ester having viscosity comparable to water. Injection was therefore very favorable. L10 has a higher dissolving power than epoxy because it is of lower viscosity. It is also more compatible with the polysulphone.
  • Fibres were found to dissolve at temperatures of 100, 110, 120, 130 and 140C with time decreasing from 20 to 3 minutes.
  • the fibre was then dissolved in a blend of L10 and epoxy MY0510 to confer phase separation.
  • the resin still injected well, cyanate ester lowering the blend viscosity, and the epoxy conferred the desired phase separation.
  • Section C - Support structure or carrier comprising soluble fibre and 2 component resin matrix (thermoset and thermoplast polymer)
  • Micrographs were produced from a hot stage microscope, which follows the dissolution of a single PES:PEES fibre dispersed in a 40:60 PES:PEES/epoxy resin, the PES:PEES content was about 10 to 15%. After dissolution the field of view was adjusted to look at the bulk sample. After 30 minutes at 175°C a noticeable particulate phase separation was observed.
  • Section D Support structure or carrier comprising Soluble fibre and Structural fibre: configurations
  • Example D2 Use of soluble fibres as stitching thread in non crimp fabrics
  • Soluble thread is stitched into carbon fibres as non crimped fabric in known manner as shown in Figure D2. When used in a curable composition the stitches dissolve giving a smooth non-crimped finish.
  • Fibres were used as upper and lower thread, with stitching speed of around 1200 stitches/min. Fibres were placed along the structural C fibres, and were also placed around circular and rectangular cut outs etc. Configurations are shown in Figure D3.
  • Figure D4 shows a preform having several fabrics coassembled
  • Example D5 Stiffening of woven fabrics using soluble fibre
  • Figure D5 shows a panel in which cross stitching is placed to stiffen a low weight 5 harness satin fabric in order to stabilise it when subjected to shear during handling.
  • Example D6 Use of soluble fibres stitch as folding seams for preforms
  • Figure D6 shows a panel which is stitched to form seams for folding in preform shaping and assembly
  • Figures D7 a to c show hybrid woven fabrics of carbon fibre with PES:PEES yarn.
  • Section E - Support structure or carrier comprising soluble and structural fibres and matrix resin
  • Figures E1 a-c show solubility of soluble PES:PEES stitching compared to polyester stitching in multiaxial fabrics. Panels were made using the same fabric style/weight stitched with polyester and PES:PEES 60 Tex fibres and alternating the layers (one with polyester stitch, one with PES:PEES stitch etc). The panels were subjected to elevated temperature of 125C with hold for dissolution to take place.
  • Example E2 Comparison or fibres solubility at different temperature
  • Figures E2a and E2b show dissolution by SEM taken through cross sections of lamina of 10 plies laid up in [0,90] configuration, each lamina being yarns or polysulphone fibre cowoven in weft direction on both sides of a C tow, injected with epoxy resin and cured with hold at different temperatures then post cured. Hold at 105C shows incomplete dissolution whereas at 135C the fibre is completely dissolved without visible trace.
  • Section F - Support structure or carrier comprising soluble and structural fibre and 2 component resin matrix (thermoset and thermoplast)
  • Example F1 Controlling amount of fibres in a support structure or carrier.
  • An amount of continuous, chopped or woven soluble fibres may be preweighed and laid up in desired manner with structural fibres and/or matrix according to the invention, providing a desired amount of polymer derived from the soluble fibres.
  • the present example illustrates calculation of fibre incorporation in the case of stitching or weaving structural fibres as hereinbefore defined, to ensure desired total amount of soluble fibre form flexible polymer element.
  • a curable composition comprising coweave or polysulphone fibre and structural fibre is prepared.
  • the resultant cured composite is required to comprise 35% matrix resin comprising epoxy resin and PES:PEES resin together with 65% structural carbon fibre.
  • These proportions are distributed in the curable composition to comprise 25% matrix resin comprising the same amount of epoxy and 10wt% less of PES:PEES, together with 75wt% of structural carbon and PES:PEES soluble fibre, in proportion 65:10 which corresponds to percentage 100:16.
  • the parameter (tows/cm) of the weaving machine is set to provide the desired Tex fpe as calculated.
  • the epoxy or epoxies in amount shown in Table FII were warmed, at temperature not exceeding 60°C. 40:60 PES:PEES copolymer with primary amine termination, 12K, was synthesised by reacting 1 mol of DCDPS with 2 moles of m-aminophenol using potassium carbonate as the catalyst and sulpholane as the reaction solvent. The polyaromatic, dissolved in a small amount of dichloromethane, was then added in corresponding amount shown in Table FII. Once the resins had been warmed and their viscosity reduced the solvent was removed at 60°C. The resin was used immediately or cooled for later use.
  • a mesh of reinforcing fibre and polysulphone fibre obtained by the method of Examples above, in respective amounts shown in Table FII was impregnated with the resin to give a total composition having the content Table FII RESIN PART A Epoxies and curing agent 17.5% PART B1 Predissolved polysulphone 10.5% REINFORCEMENT PART B2 Polysulphone fibres 7% PART C Carbon 65%
  • a hybrid textile reinforcement configuration for example woven fabric or a multiaxial fabric was used eg as illustrated in Figure F2.
  • Example F3 Infusion of support structure or carrier with curable component
  • Example F2 The composites obtained in Example F2 were subject to elevated temperature for dissolution of fibres, and on dissolution were subject to further elevated temperature for curing.
  • Figure F4a shows dissolution of polysulphone fibres in the above system with different amounts of polysulphone (from 0 to 30%).
  • the graph shows that the dissolution occurs also for high level of polysulphone.
  • the slightly higher dissolution times for higher concentrations of polysulphone are due only to the higher viscosity.
  • thermoplastic 50% thermoplastic would cause a definite improvement in properties like toughness.
  • thermoplastic An increase in the level of thermoplastic leads to an improvement in toughness properties like Gc and Kc as reported in the following Table.
  • the pressurized atmosphere is commonly about 560kPa - 690 kPa (85 psi - 100 psi).
  • the entire operation of the autoclave is computer controlled.
  • VARTM simplifies hard mold RTM by employing only one-sided moulds, and using vacuum bagging techniques to compress the preform. Resin injection is driven by the 1 atm pressure difference between the mould cavity and the resin source but mould filling times can be far too long, and resin does can cure before total fill.
  • RIFT provides a 'distribution media', being a porous layer having very low flow resistance, provides the injected resin with a relatively easy flow path. The resin flows quickly through the distribution media, which is placed on the top of the laminate and then flows down through the thickness of the preform.
  • the method of the invention consists of using an hybrid fabric containing structural fibres (carbon, glass, aramid etc) and polysulphone multifilament having a count between 30 and 160 tex composed of single fibres having a diameter between 30 and 80 micron as shown in the Figure G1a.
  • the structural fibres for example carbon fibres, have usually diameters around 6-7 micron and are therefore smaller than the above polysulphone fibres. This difference in diameter creates artificial 'channels' that facilitate the injection and also the subsequent air removal from the laminate.
  • the fabrics have been cut in various rectangular shapes with a size of 6x4 in and laid following the lay-up [0,90]8 to produce composite laminate using a RIFT process.
  • Figure G2 shows the RIFT equipment that has been used for the example.
  • the yellow fabric is the flow distribution media used to infuse the resin.
  • the T connector constitutes the gate and the vent and their shape creates a stable flow front.
  • a resin with the following formulation was injected: % PY306 36.86 MY0510 35.42 44'DDS 27.72
  • Figures G2 c and G2 d are taken from the panel B i.e. the panel manufactured with the hybrid carbon / polysulphone fibres: In this case, even if the panels have been cured without pressure is not possible to see any voids.

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  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
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  • Health & Medical Sciences (AREA)
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  • Reinforced Plastic Materials (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Moulding By Coating Moulds (AREA)
  • Nonwoven Fabrics (AREA)
  • Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
  • Artificial Filaments (AREA)
  • Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
  • Laminated Bodies (AREA)

Claims (10)

  1. Härtbare Zusammensetzung, die ein flexibles Polymerelement und eine Harzmatrixkomponente umfasst, wobei das flexible Polymerelement in der festen Phase vorliegt und so ausgelegt ist, dass es durch Auflösen bei Kontakt mit der Harzmatrixkomponente der härtbaren Zusammensetzung, in der das Polymer löslich ist, bei einer Temperatur, die niedriger ist als die Temperatur des Beginns der Gelierung und/oder Härtung der härtbaren Zusammensetzung, zumindest teilweise einen Phasenübergang in die flüssige Phase vollzieht, dadurch gekennzeichnet, dass der Phasenübergang zur flüssigen Phase durch Auflösen des löslichen Polymers in der Harzmatrixkomponente erfolgt,
    wobei das Matrixharz härtbar ist und aus der Gruppe bestehend aus einem Epoxidharz, einem Polyadditionsharz, insbesondere einem Bismaleimidharz, einem Formaldehydkondensatharz, insbesondere einem Formaldehyd-PhenolHarz, einem Cyanatharz, einem Isocyanatharz, einem Phenolharz und Mischungen aus zwei oder mehr davon ausgewählt ist,
    und
    wobei das flexible Polymerelement mindestens ein polyaromatisches Sulfon umfasst, das Ether-verknüpfte Wiederholeinheiten umfasst, gegebenenfalls zusätzlich Thioether-verknüpfte Wiederholeinheiten umfasst, wobei die Einheiten bestehen aus

            -(PhAPh)n-

    und

            -(Ph)a-

    wobei A=CO oder SO2, Ph Phenylen ist, n = 1 bis 2, a = 1 bis 4, bevorzugt a = 1, 2 oder 3 und eine gebrochene Zahl sein kann, und wenn a größer 1 ist, die Phenylene über eine chemische Einfachbindung oder eine andere zweiwertige Gruppe als -CO- oder -SO2- linear verknüpft sind oder direkt oder über eine cyclische Komponente wie eine Säurealkylgruppe, ein (hetero)aromatisches oder cyclisches Keton, Amid, Imid, Imin aneinander ankondensiert sind; und
    wobei das flexible Polymerelement in Form einer Einzel- oder Mehrfachfaser, eines Filaments, Bands oder von Mischungen oder eines Bindungsmusters daraus vorliegt.
  2. Härtbare Zusammensetzung nach Anspruch 1, wobei die Einheiten in dem Polyarylsulfon der flexiblen Polymerelemente
    X Ph SO2 Ph X Ph SO2 Ph ("PES") und (I)
    X(Ph)a XPh SO2 Ph ("PEES") (II)
    sind, wobei X O oder S ist und sich von Einheit zu Einheit unterscheiden kann; das Verhältnis von I zu II (jeweils) bevorzugt zwischen 10:90 und 80:20 liegt.
  3. Härtbare Zusammensetzung nach Anspruch 1 oder 2, wobei die polyaromatische Verbindung Seiten- oder Endgruppen enthält, die ausgewählt sind aus OH, NH2, NHR' oder -SH, wobei R' eine Kohlenwasserstoffgruppe ist, die bis zu 8 Kohlenstoffatome enthält, Epoxy, (Meth)acrylat, Cyanat, Isocyanat, Acetylen oder Ethylen, wie in Vinyl, Allyl oder Maleimid, Anhydrid, Oxazolin und Monomeren mit Sättigung.
  4. Härtbare Zusammensetzung nach einem der Ansprüche 1 bis 3, die zusätzlich ein thermoplastisches Polymer umfasst, das ausgewählt ist aus Cellulosederivaten, Polyester, Polyamid, Polyimid, Polycarbonat, Polyurethan, Polyacrylonitril, Poly(methylmethacrylat), Polystyrol und polyaromatischen Verbindungen wie Polyarylethern, Polyarylketonen und insbesondere Polyarylsulfonen; Copolymere ausgewählt aus Polyesteramid, Polyamidimid, Polyetherimid, Polyaramid, Polyarylat, Poly(ester)carbonat, Poly(methylmethacrylat/butylacrylat), Polyethersulfon-Etherketon; und Polymermischungen daraus.
  5. Härtbare Zusammensetzung nach einem der Ansprüche 1 bis 4, die ferner zusätzliche Verstärkungsfasern, Katalysatoren, Härter, Zusatzstoffe wie Füllstoffe und Ähnliches umfasst.
  6. Härtbare Zusammensetzung nach Anspruch 5, wobei das flexible Polymerelement so ausgelegt ist, dass es beim Härten der härtbaren oder teilweise Phasentrennung vollzieht und so ein zweiphasiges Matrixharzsystem entsteht.
  7. Härtbare Zusammensetzung nach einem der vorhergehenden Ansprüche, wobei ein thermoplastisches Harz in einer ersten Menge in flüssiger Phase als Matrixkomponente vorliegt und zusätzlich in einer zweiten Menge in Form des mindestens einen flexiblen Polymerelements in fester Phase vorliegt.
  8. Verfahren zur Herstellung einer härtbaren Zusammensetzung nach Anspruch 5 bis 7, das ein Kontaktieren eines flexiblen Polymerelements oder einer Trägerstruktur mit Harzmatrix umfasst, beispielsweise durch Tränken, Injektion oder Infusion, Mischen und Ähnliches.
  9. Verfahren nach Anspruch 8, wobei die Injektion bei Umgebungstemperatur oder einer höheren Temperatur unter der Auflösungstemperatur erfolgt, zweckmäßig im Bereich Raumtemperatur bis 100°C, damit eine zweckmäßige Harzviskosität erreicht wird.
  10. Verfahren nach Anspruch 8 oder 9, wobei die Injektion unter Verwendung eines Sacks, eines Dorns und/oder einer Form und gegebenenfalls unter Verwendung von Kanälen oder Ähnlichem zur Fließunterstützung erfolgt, wobei die Injektionsdauer im Bereich von 2 bis 300 Minuten, vorzugsweise 2 bis 120 Minuten liegt.
EP06076672.2A 2000-08-22 2001-08-16 Flexible Polymergegenstände zur Änderung der Zähigkeit eines Prepregs Expired - Lifetime EP1754743B1 (de)

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GB0020630A GB0020630D0 (en) 2000-08-22 2000-08-22 Support structure or carrier for a curable composition
GB0104947A GB0104947D0 (en) 2001-02-28 2001-02-28 Composition comprising elevated levels of a component polymer
PCT/GB2001/003655 WO2002016481A1 (en) 2000-08-22 2001-08-16 Flexible polymer element as toughening agent in prepregs
EP01958213A EP1317501B1 (de) 2000-08-22 2001-08-16 Flexibles polymerelement zur erhöhung der festigkeit von prepregs

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ES2806992T3 (es) 2021-02-19
NO20030782L (no) 2003-04-15
NO20030782D0 (no) 2003-02-19
CN1468279A (zh) 2004-01-14
MXPA03001412A (es) 2005-09-20
AU2007203150A1 (en) 2007-07-26
EP1317501B1 (de) 2006-11-22
AU2007203150B8 (en) 2009-08-27
MY136891A (en) 2008-11-28
RU2272051C2 (ru) 2006-03-20
JP5033300B2 (ja) 2012-09-26
CA2420331A1 (en) 2002-02-28
KR100849289B1 (ko) 2008-07-29
BR0113446A (pt) 2003-07-01
TWI233442B (en) 2005-06-01
US20090151860A1 (en) 2009-06-18
JP2004506799A (ja) 2004-03-04
NO336285B1 (no) 2015-07-13
DE60124745T2 (de) 2007-09-13
AU2001279940A1 (en) 2002-03-04
AU2007203150B2 (en) 2009-07-30
EP1317501A1 (de) 2003-06-11
ES2272518T3 (es) 2007-05-01
DE60124745D1 (de) 2007-01-04
WO2002016481A1 (en) 2002-02-28
EP1754743A1 (de) 2007-02-21
KR20030029838A (ko) 2003-04-16
IL154576A0 (en) 2003-09-17
ATE346107T1 (de) 2006-12-15
CN100575397C (zh) 2009-12-30

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